HydrALAZINE Hydrochloride
- Product NDC
- 70518-2091
- 11-digit product format
- 705182091
- Labeler code
- 70518
- Product ID
- 70518-2091_972116f4-cc77-b6b2-e053-2995a90ae449
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HydrALAZINE Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA200770
- Marketing category
- ANDA
- Marketing start
- 2019-05-21
- Marketing end
- 0000-00-00
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record